$0.00
Shopping Cart
Facebook-f Instagram
DONATE
Donate

Clinical Trial Record

Return to Clinical Trials

Chemotherapy, Interferon Alfa, and Radiation Therapy in Treating Patients Who Have Undergone Surgery For Pancreatic Cancer

2002-05

2010-12

2010-12

29

Study Overview

Chemotherapy, Interferon Alfa, and Radiation Therapy in Treating Patients Who Have Undergone Surgery For Pancreatic Cancer

RATIONALE: Drugs used in chemotherapy, such as cisplatin and fluorouracil, use different ways to stop tumor cells from dividing so they stop growing or die. Biological therapies such as interferon alfa may interfere with the growth of the tumor cells and slow the growth of cancer. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining chemotherapy and interferon alfa with radiation therapy after surgery may kill any remaining tumor cells. PURPOSE: This phase II trial is studying how well giving cisplatin, fluorouracil, and interferon alfa together with radiation therapy works in treating patients who have undergone surgery for stage I, stage II, or stage III pancreatic cancer.

OBJECTIVES: Primary * Determine the overall survival of patients with previously resected pancreatic adenocarcinoma treated with postoperative cisplatin, interferon alfa, fluorouracil, and concurrent radiotherapy. * Determine the toxic effects of this regimen in these patients. Secondary * Determine the disease-specific, biochemical failure-free, and symptom/treatment-free survival of patients treated with this regimen. * Determine the quality of life of patients treated with this regimen. OUTLINE: * Chemoradiotherapy: Patients receive fluorouracil intravenous (IV) continuously and interferon alfa subcutaneously (SQ) 3 times per week (total of 17 doses) on days 1-19 and 29-45 and cisplatin IV over 6 hours on days 1, 8, 15, 29, 36 and 43. Patients also undergo concurrent radiotherapy once daily, 5 days a week in weeks 1-3 and 5-7 (28 fractions). * Post-chemoradiotherapy fluorouracil: Patients receive fluorouracil IV continuously on days 71-108 and 127-168. PROJECTED ACCRUAL: A total of 44 patients will be accrued for this study.

  • Pancreatic Cancer
  • BIOLOGICAL: Recombinant Interferon Alfa
  • DRUG: Cisplatin
  • DRUG: Fluorouracil
  • RADIATION: Radiation Therapy
  • ID02-040
  • P30CA016672 (U.S. NIH Grant/Contract)
  • MDA-ID-02040 (OTHER Identifier) (OTHER: UT MD Anderson Cancer Center)
  • CDR0000327752 (REGISTRY Identifier) (REGISTRY: NCI PDQ)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates Results Reporting Dates Study Record Updates

2003-09-10  

2012-01-23  

2012-02-13  

2003-09-10  

2012-01-23  

2012-02-15  

2003-09-11  

2012-02-14  

2012-02  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
Treatment

Allocation:
Na

Interventional Model:
Single Group

Masking:
None

Arms and Interventions

Participant Group/ArmIntervention/Treatment
EXPERIMENTAL: Postoperative Chemoradiation Regimen

Postoperative Cisplatin 30 mg/m^2 intravenous (IV) weekly for 6 doses, Interferon Alfa-2b 3 million units subcutaneous (SQ) on Monday, Wednesday and Friday days 1-19 and 29-45 for 17 total doses, and 5-fluorouracil (5-FU) 175 mg/m2/day by continuous intra

BIOLOGICAL: Recombinant Interferon Alfa

  • 3 million units subcutaneously every other day (Monday, Wednesday and Friday) during Days 1-19 and 29-45, for 6 1/2 weeks totaling 17 doses.

DRUG: Cisplatin

  • 30 mg/m^2 IV over 60 minutes on days 1, 8, 15, 29, 36, 43 - weekly for total 6 doses, during 5 1/2 weeks radiation therapy.

DRUG: Fluorouracil

  • 175 mg/m^2/day continuous infusion over 6 1/2 weeks for total 3 courses: Days 1-19 and 29-45, Days 71-108 and Days 127-168.

RADIATION: Radiation Therapy

  • External beam radiation on days 1-19 and days 29-45, 9 day treatment break on day 20.
Primary Outcome MeasuresMeasure DescriptionTime Frame
Median Overall Survival (OS)Overall Survival defined overall survival time, measured from date of tissue diagnosis till disease progression or death.Participants followed till disease progression or death (approximately 6 years)
Secondary Outcome MeasuresMeasure DescriptionTime Frame

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

    Inclusion Criteria:
    1. Biopsy proven completely resected (R0 or R1) pancreatic adenocarcinoma of the pancreatic head or uncinate process [American Joint Committee on Cancer (AJCC) Stage I-III]. Surgery (pancreaticoduodenectomy) may be performed at M. D. Anderson Cancer Center or prior to referral to M. D. Anderson Cancer Center. Protocol treatment must begin within 12 weeks of surgery. 2. Postoperative (pre-treatment) computed tomography (CT) scan without evidence of radiographically defineable residual primary/metastatic disease or clinically significant post-surgical changes. 3. Staging studies completed within three weeks +/- 3 days of protocol registration. 4. Hemoglobin (Hb) >9.0 g/%, White Blood Count (WBC) >3,000 cells/mm3 (Absolute neutrophil count (ANC)>1,500 cells/mm3), platelets >75,000 cells/mm3. 5. Postoperative serum calcium (CA) 19-9 < 100. 6. Performance status: Zubrod 0 or 1. 7. Creatinine £1.5 mg/dL and calculated or measured creatinine clearance (CrCl) of 60 ml/min or greater by the following formula: Creatinine clearance rate (CrCl) = (140 - age)
  • Weight (kg)
  • 0.85 (female) OR
  • 1.00 (male) 72
  • serum creatinine 8. Patients should have bilateral renal function, as determined on excretory urogram (IVP) or abdominal CT, or ³ 2/3 of one functioning kidney must be able to be shielded from the radiation beam. 9. No acute infections at the time of therapy initiation. 10. Women of childbearing potential must agree to practice adequate contraception and to refrain from breast feeding, as specified in the informed consent. 11. Patients must sign a study-specific consent form, which is attached to this protocol. 12. Patients with a prior history of non-pancreatic malignancy who are free of disease from their primary cancer may be eligible at the discretion of the study chair.

    • Exclusion Criteria:
    1. Residual (clinical or CT definable) metastatic or incompletely resected local disease. 2. Patients with positive peritoneal cytology (for adenocarcinoma) detected at laparotomy for pancreaticoduodenectomy or as part of prior laparoscopic assessment of peritoneal cytology. 3. Patients with a history of hypersensitivity to interferon alfa-2b. 4. Patients with significant cardiovascular disease, such as unstable angina or congestive heart failure. 5. Pregnancy or breastfeeding. 6. Patients with severe pulmonary disease. 7. Children under the age of 18 are excluded (as the disease is rare and toxicity profile of this regimen untested in pediatric patients). 8. Presence or history of severe depression.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

  • National Cancer Institute (NCI)
  • Schering-Plough
  • STUDY_CHAIR: Peter W. Pisters, MD, M.D. Anderson Cancer Center

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

No publications available

NPCF Pop up

Make-A-Will Month

Snag 6508be92
Learn More
Donate Now Online
Other Ways to Donate